Skip to main content
Fig. 6 | BMC Veterinary Research

Fig. 6

From: A frameshift mutation in MOCOS is associated with familial renal syndrome (xanthinuria) in Tyrolean Grey cattle

Fig. 6

Summary of known bovine and human MOCOS mutations. a The two bovine MOCOS transcripts (MOCOS-201 and MOCOS-202) are shown (center). The position of the mutation detected in Tyrolean Grey cattle is indicated. The two possible wild type proteins and the relevant domains (AAT: aspartate aminotransferase; MBB: mosc beta barrel; MOSC: MOSC domain) are shown above. Below, the two predicted mutant proteins are shown. Note the predicted mutant truncated proteins lack MBB and MOSC domains. b Previously reported mutations causing xanthinuria in human and cattle are displayed (JB: Japanese Black cattle; TG: Tyrolean Grey cattle). The nature of the predicted mutation effect of the protein is shown. The positions of mutated bovine residues are aligned to the length of the human protein

Back to article page